Evidence map›Paper›PMID 28781947›Full record

ArticleFEBS open bio2017

Structural flexibility of human α-dystroglycan.

Sonia Covaceuszach, Manuela Bozzi, Maria Giulia Bigotti, Francesca Sciandra, Petr Valeryevich Konarev, Andrea Brancaccio, Alberto Cassetta

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. A molecular overview of the primary dystroglycanopathies.Journal of cellular and molecular medicine · 2019
    Review
  9. Neurexins - versatile molecular platforms in the synaptic cleft.Current opinion in structural biology · 2019
    Review
  10. Article
  11. Article
4 · The record

Corrections and comments

  • Commented on by
    2017
5 · Who and what money

Authors and funding

7 authors at 5 institutions in 3 countries.

Sonia CovaceuszachIstituto di Cristallografia CNR, Trieste Outstation Italy.
Manuela BozziIstituto di Biochimica e Biochimica Clinica Università Cattolica del Sacro Cuore Roma Italy.
Maria Giulia BigottiSchool of Biochemistry University of Bristol UK.
Francesca SciandraIstituto di Chimica del Riconoscimento Molecolare CNR c/o Università Cattolica del Sacro Cuore Roma Italy.
Petr Valeryevich KonarevShubnikov Institute of Crystallography of Federal Scientific Research Centre "Crystallography and Photonics" of Russian Academy of Sciences Moscow Russia.
Andrea BrancaccioIstituto di Chimica del Riconoscimento Molecolare CNR c/o Università Cattolica del Sacro Cuore Roma Italy.
Alberto CassettaIstituto di Cristallografia CNR, Trieste Outstation Italy.
Institute of Crystallography · ITUniversity of Bristol · GBA.V. Shubnikov Institute of Crystallography · RUInstitute of Chemistry of Molecular Recognition · ITUniversità Cattolica del Sacro Cuore · IT

Funding

Wellcome Trust
6 · The paper itself

Abstract

Dystroglycan (DG), composed of α and β subunits, belongs to the dystrophin-associated glycoprotein complex. α-DG is an extracellular matrix protein that undergoes a complex post-translational glycosylation process. The bifunctional glycosyltransferase like-acetylglucosaminyltransferase (LARGE) plays a crucial role in the maturation of α-DG, enabling its binding to laminin. We have already structurally analyzed the N-terminal region of murine α-DG (α-DG-Nt) and of a pathological single point mutant that may affect recognition of LARGE, although the structural features of the potential interaction between LARGE and DG remain elusive. We now report on the crystal structure of the wild-type human α-DG-Nt that has allowed us to assess the reliability of our murine crystallographic structure as a α-DG-Nt general model. Moreover, we address for the first time both structures in solution. Interestingly, small-angle X-ray scattering (SAXS) reveals the existence of two main protein conformations ensembles. The predominant species is reminiscent of the crystal structure, while the less populated one assumes a more extended fold. A comparative analysis of the human and murine α-DG-Nt solution structures reveals that the two proteins share a common interdomain flexibility and population distribution of the two conformers. This is confirmed by the very similar stability displayed by the two orthologs as assessed by biochemical and biophysical experiments. These results highlight the need to take into account the molecular plasticity of α-DG-Nt in solution, as it can play an important role in the functional interactions with other binding partners.

Indexed as

conformational stabilitymuscular dystrophysmall‐angle X‐ray scatteringstructural flexibilityX‐ray crystal structureα‐Dystroglycan

Identifiers

PMID28781947
PMCPMC5537065
OpenAlexW2683645756

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.